Salivary Gland Tumors
Basics
Salivary gland tumors consist of benign or malignant neoplasms of the major and minor salivary glands. Tumors may be mimicked clinically by a variety of inflammatory or infectious disorders:
- Major: parotid, submaxillary, sublingual glands
- Minor: intraoral, pharyngeal, and nasal glands (600 to 1,000 glands distributed throughout the upper aerodigestive tract)
Description
- Adult neoplasms
- Benign: pleomorphic adenoma, Warthin tumor (adenolymphoma), oncocytoma, and monomorphic adenoma
- Malignant: mucoepidermoid carcinoma, adenoid cystic carcinoma, acinic cell carcinoma, carcinoma ex pleomorphic adenoma, squamous cell carcinoma (SCC), adenocarcinoma
- Total distribution of salivary gland neoplasms by type
- Pleomorphic adenoma (most common): 45% overall
- Monomorphic adenoma: 12% overall
- Mucoepidermoid carcinoma: 12% overall
- Adenoid cystic carcinoma: 6% overall
- Remaining neoplasms: 25% overall
- Distribution: parotid (80%); submandibular (10–15%); sublingual and minor (5–10%)
- Parotid (80% benign; 20% malignant)
- Pleomorphic adenoma: 60%
- Monomorphic adenoma: 8%
- Warthin tumor: 8%
- Mucoepidermoid carcinoma: 12%
- Adenoid cystic carcinoma: 5%
- Adenocarcinoma and SCC: 5%
- Submandibular (60% benign; 40% malignant)
- Pleomorphic adenoma: 40%
- Mucoepidermoid carcinoma: 10%
- Adenoid cystic carcinoma: 20%
- Lingual and minor salivary glands (40% benign; 60% malignant)
- Pleomorphic adenoma: 40%
- Mucoepidermoid carcinoma: 25%
- Adenoid cystic carcinoma: 25%; generally, as the size of the gland decreases, the incidence of malignancy increases.
- Parotid (80% benign; 20% malignant)
- Pediatric neoplasms
- These tumors are most frequently benign but may be malignant.
Epidemiology
Incidence
- 1.5/100,000 cases in individuals in the United States
- ~700 deaths annually
- Median age
- Benign: 45 years
- Malignant: 60 years
- Gender predilection
- Benign: female > male
- Malignant: male = female
Prevalence
Etiology and Pathophysiology
Etiology and pathophysiology not fully understood; certain pathways and oncogenes have been implicated: p53, Bcl-2, PI3K/Akt, MDM2, VEGF, HGF, and ras.
- Predominant/bicellular theory: Tumors arise from either the secretory duct reserve cell or the intercalated duct reserve cell.
- Multicellular theory: Tumors arise from several cell types of origin within the salivary gland unit.
Genetics
Increased incidence of adenocarcinoma of parotid in Eskimos; otherwise, no known genetic pattern
Risk Factors
- Tobacco and alcohol abuse associated with Warthin tumor
- Alcohol increases likelihood ratio by 2:1.
- Radiation has shown a 4-fold increased dose-related response in salivary gland cancer 15 to 20 years after treatment. Increased risk has also been reported in atomic bomb survivors.
- EBV has been associated with lymphoepithelial carcinoma in Asians, but there is no evidence of causal association in other tumors.
- Silica dust has been associated with a 2.5-fold increase in salivary gland neoplasia.
- Kerosene-cooking fuel exposure
- Nitrosamine exposure in rubber workers
- Early menarche and nulliparity
General Prevention
Cessation of tobacco and alcohol use
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